N'-甲基-2-吡啶甲酰肼 | 34955-20-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: N'-甲基-2-吡啶甲酰肼
• 英文名称: N'-methylpicolinohydrazide
• 英文别名: pyridine-2-carboxylic acid-(N'-methyl-hydrazide)；Pyridin-2-carbonsaeure-(N'-methyl-hydrazid)；1-Picolinoyl-2-methylhydrazin；2-Pyridinecarboxylic acid, 2-methylhydrazide；N'-methylpyridine-2-carbohydrazide
• CAS: 34955-20-9
• 化学式: C₇H₉N₃O
• 分子量: 151.168
• InChiKey: WDAOXBJPCRPNTD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.3
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  54
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N'-甲基-2-吡啶甲酰肼 、 Morpholinodithiocarbaminsaeure-methylester 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 吡啶 为溶剂， 反应 2.5h， 以52%的产率得到1-methyl-4-morpholino-3-(pyridine-2-yl)-1H-1,2,4-triazole-5(4H)-thione
  参考文献：
  名称：

  Synthesis and Tuberculostatic Activity of Novel 1,2,4-Triazoles Obtained from Heterocyclic Carbohydrazides

  摘要：

  The novel 1,2,4-triazole derivatives have been synthesized by a few different pathways. Heterocyclic carbohydrazides were used to obtain monoesters of hydrazine acids (1-6), thiosemicarbazide derivatives (7-17), and finaly 1,2,4-triazole-5-thiones (18-38). Carbohydrazides were also cyclized with methyl carbamodithioates in the presence of DBU giving 1,2,4-triazole-5-thiones (18, 19, 39-47). Two of final products (39, 40) were undergone alkylation in alkaline solution to appropriate sulfides (48-53). Then methylsulfides (48, 49) were oxidized with peroxyacetic acid to sulfoxides (54, 55). The obtained compounds were tested in vitro towards Mycobacterium tuberculosis.

  DOI：

  10.3987/com-09-11888
• 作为产物：
  描述：

  甲基肼 、 alkaline earth salt of/the/ methylsulfuric acid 生成 N'-甲基-2-吡啶甲酰肼
  参考文献：
  名称：

  Shimizu et al., Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1952, vol. 72, p. 1639,1641

  摘要：

  DOI：

文献信息

• Heterocyclic compounds having inhibitory activity against HIV integrase
  申请人：Murai Hitoshi

  公开号：US20090118233A1

  公开（公告）日：2009-05-07

  A heterocyclic compound of the formula (I): wherein B 1 is —C(R 2 )═ or —N═; R 1′ is H, etc.; one of R 1 and R 2 is -Z 1 -Z 2 -Z 3 -R 5 wherein Z 1 and Z 3 are independently single bond, optionally substituted alkylene, etc.; Z 2 is single bond, optionally substituted alkylene, etc.; R 5 is optionally substituted aryl, optionally substituted heteroaryl, etc., and the other of R 1 and R 2 is H; -A 1 - is —C(—Y)═C(—R A )—C(—R 3 )═C(—R 4 )—, etc. wherein Y is OH, etc.; R A is —COR 7 wherein R 7 is OH, etc.; one of R 3 and R 4 is carboxy, etc., and the other of R 1 and R 2 is H, etc, a prodrug thereof, a pharmaceutically acceptable salt thereof, and a solvate thereof, having an antiviral activity, more particularly, an inhibitory activity against HIV integrase, and a pharmaceutical composition containing the same, especially an anti-HIV drug.

  一种具有以下式（I）的杂环化合物：其中B1为—C（R2）═或—N═；R1'为H等；R1和R2中的一个为-Z1-Z2-Z3-R5，其中Z1和Z3分别为单键，可选择性地取代的烷基等；Z2为单键，可选择性地取代的烷基等；R5为可选择性取代的芳基，可选择性取代的杂环芳基等；R1和R2中的另一个为H；-A1-为—C（—Y）═C（—RA）—C（—R3）═C（—R4）—等，其中Y为OH等；RA为—COR7，其中R7为OH等；R3和R4中的一个为羧基等，另一个为H等。该化合物的前药、其药学上可接受的盐和溶剂化物具有抗病毒活性，尤其是对HIV整合酶的抑制活性，并且包含该化合物的药物组合物，特别是一种抗HIV药物。
• BIELAK, LIDIA;MISIUNA, DIWA;BILINSKI, STANISLAW, ANN. UMCS. D, 42,(1987) C. 5-15
  作者：BIELAK, LIDIA、MISIUNA, DIWA、BILINSKI, STANISLAW

  DOI：——

  日期：——
• Synthesis and anti-prion aggregation activity of acylthiosemicarbazide analogues
  作者：Dong Hwan Kim、Jaehyeon Kim、Hakmin Lee、Dongyun Lee、So Myoung Im、Ye Eun Kim、Miryeong Yoo、Yong-Pil Cheon、Jason C. Bartz、Young-Jin Son、Eun-Kyoung Choi、Yong-Sun Kim、Jae-Ho Jeon、Hyo Shin Kim、Sungeun Lee、Chongsuk Ryou、Tae-gyu Nam

  DOI：10.1080/14756366.2023.2191164

  日期：2023.12.31
• POLYENE MACROLIDE DERIVATIVE
  申请人：Shionogi & Co., Ltd.

  公开号：US20170190729A1

  公开（公告）日：2017-07-06

  The present invention is the following Amphotericin B derivative: wherein each symbol is defined in description. The compound of the present invention has 16th position (X) is urea structure, cyclic structure, hydroxyalkyl or substituted monoalkylcarbamoyl. The compound of the present invention has antifungal activity.
• US7358249B2
  申请人：——

  公开号：US7358249B2

  公开（公告）日：2008-04-15